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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373414Generated: October 26, 2026

tert-butyl N-(prop-2-yn-1-yl)carbamate → HCID 59851457, compound

https://huagongshe.com/reaction/2373414

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
Reactant9-Chloro-2-(3-iodo-phenylamino)-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-oneHCID 59851283—
ReactantHCID 66934682HCID 66934682—
ProductHCID 59851457HCID 59851457—

Reaction Steps

In a manner similar to that described for Method O, 9-chloro-2-(3-iodo-phenylamino)-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-58) and tert-butyl prop-2-ynylcarbamate was converted to {3-[3-(9-chloro-6-oxo-6,7-dihydro-5H-benzo[b]pyrimido[4,5-d]azepin-2-ylamino)-phenyl]-prop-2-ynyl}-carbamic acid tert-butyl ester, which was subsequently deprotected according to Method K to give I-67 (62%): HRMS Calcd. for C21H16ClN5O: 390.1121, Found 390.1117.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459448B2
Source datasetuspto-grants-2008_12
ORD IDord-7a1bc298d8a34c9db40cc2f7bed97878
Source noteuspto-grants-2008_12