HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041005Generated: October 31, 2026
7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amine → HCID 66830680, compound
https://huagongshe.com/reaction/1041005
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-morpholino-6,7,8,9-tetrahydro-5H-benzo[7]annulen-3-amine | HCID 57416136 | — |
| Reactant | HCID 57522618 | HCID 57522618 | — |
| Product | HCID 66830680 | HCID 66830680 | — |
Reaction Steps
In an analogous procedure to Example 651, part c, 7-Morpholin-4-yl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ylamine and (1S,2S,3R,4R)-3-(2,5-Dichloro-pyrimidin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide were combined to yield 1S,2S,3R,4R)-3-[5-Chloro-2-(7-morpholin-4-yl-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-ylamino)-pyrimidin-4-ylamino]-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide as a white solid. 1H-NMR (CDCl3) δ 9.12 (s, 1H), 7.93 (s, 1H), 7.78 (s, 1H), 7.70 (m, 1H), 7.52 (m, 1H), 7.46 (d, J=21.2 Hz, 1H), 7.26 (s, 1H), 7.00 (d, J=8.2 Hz, 1H), 6.35 (s, 1H), 6.27 (s, 1H), 4.13 (m, 1H), 3.31 (s, 3H), 2.87 (s, 1H), 2.77 (s, 1H), 2.56 (m, 6H), 2.45 (m, 4H), 2.10 (d, J=8.6 Hz, 1H), 1.95 (m, 2H), 1.40 (d, J=8.8 Hz, 1H), 1.31 (m, 2H). LC/MS (ESI+)=509 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552186B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-693111492a704ac3b55b5501e5920181 |
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| Source note | uspto-grants-2013_10 |
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