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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898336Generated: October 30, 2026

2-Chloropyrimidine → HCID 11417002, compound

https://huagongshe.com/reaction/898336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
ReactantHCID 59691864HCID 59691864—
ProductHCID 11417002HCID 11417002—

Reaction Steps

2-Bromo-N-pyrimidin-2-yl-5,6,7,8,9,10-hexahydrocyclohepta[b]indol-6-amine was prepared from 2-bromo-5,6,7,8,9,10-hexahydrocyclohepta[b]indol-6-amine (150 mg, 0.54 mmol) and 2-chloropyrimidine (123 mg, 1.07 mmol) in a similar manner as described in Example 22 to give 18 mg (9%) of a yellow solid. 1H-NMR (DMSO-d6): δ 10.80 (s, 1H), 8.31 (d, 2H), 7.57 (s, 1H), 7.49 (d, 1H), 7.20 (d, 1H), 7.07-7.04 (m, 1H), 6.60 (t, 1H), 5.36-533 (m, 1H), 2.94-2.89 (m, 1H), 2.70-2.63 (m, 1H), 2.05-1.94 (m, 2H), 1.89-1.59 (m, 4H); MS m/z (M+1) 357, 359; (M−1) 355, 357.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351733B2
Source datasetuspto-grants-2008_04
ORD IDord-80c45a07ad244f65bc7cac815e035f16
Source noteuspto-grants-2008_04