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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300617Generated: October 31, 2026

Boc-Tyr-OMe → HCID 69835491, compound

https://huagongshe.com/reaction/2300617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoc-Tyr-OMeHCID 7019130—
ReactantHCID 18376378HCID 18376378—
ProductHCID 69835491HCID 6983549194%

Reaction Steps

Intermediate 57 was prepared as described above for the preparation of intermediate 52. From 575 mg of N-(Boc)-L-Tyrosine methyl ester and 500 mg of Intermediate 9B was prepared 940 mg of BOC-protected intermediate methyl ester (94% yield; 1H NMR (DMSO-d6, 300 MHz) δ7.93 (m, 2H), 7.47-7.41 (m, 3H), 7.04 (d, 2H, J=8.4), 6.86 (d, 2H, J=8.6), 4.96 (d, 1H, J=4.56 (m, 1H), 4.34 (t, 2H, J=6.8), 3.73 (s, 3H), 3.23 (t, 2H, J=6.9), 3.04 (m, 2H), 2.90 (q, 2H, J=7.5), 1.44 (s, 9H), 1.37 (t, 3H, J=7.5)); From 900 mg of protected intermediate was prepared 900 mg of intermediate 57 as a solid. 1H NMR (DMSO-d6, 300 MHz) δ8.16 (br s, 2H), 7.85 (m, 2H), 7.5-7.43 (m, 3H), 7.14 (d, 2H, J=8.6), 6.90 (d, 2H, J=8.6), 4.27 (t, 2H, J=6.5), 4.12 (m, 1H), 3.12 (t, 2H, J=6.5), 3.0 (m, 2H), 2.86 (q, 2H, J=7.5), 1.26 (t, 3H, J=7.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498174B1
Source datasetuspto-grants-2002_12
ORD IDord-78258436c966412ab7265be0151b9f8d
Source noteuspto-grants-2002_12